Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Toxic Waste Short Circuits Bubble Gum Recall Due to Lead Levels March 28, 2011 Staff Writers Add Your CommentsA recall has been issued for Toxic Waste brand Short Circuit Bubble Gum due to high amounts of lead contained in the product, continuing a string of recalls issued by the manufacturer this year over lead concerns.ย The Toxic Waste Short Circuits Bubble Gum recall was announced on March 26 for one lot of the product made by Candy Dynamics. The recall came after the FDA tested the gum and found it had elevated lead levels of 0.189 parts per million (ppm); nearly twice the regulatory limit of 0.1 ppm for lead.The bubble gum recall affects Toxic Waste Short Circuits Bubble Gum in the 3.2 oz size, with Lot #15070SC12. The candy was distributed nationwide from January 4, 2011, until March 18. It has a UPC of 0 89894 31001 3.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONIn January, Candy Dynamics issued a recall for all of its Toxic Waste brand Nuclear Sludge chew bars due to elevated lead levels, which were as high as 0.24 ppm. Later that month, theย Nuclear Sludgeย recall was expanded to include everything under the Nuclear Sludge label, including both chew bars and candy pieces, after testing found other products with lead levels as high as .311 ppm. The company canceled that candy line.Currently, Candy Dynamics says it intends to continue selling Short Circuits Bubble Gum, and the recall is limited to just the one lot that was detected as having high lead levels.The U.S. Centers for Disease Control and Prevention (CDC) consider 10 milligrams of lead per deciliter of blood to be the level of concern for exposure to lead. The CDC estimates that approximately 250,000 children in the U.S. have blood lead levels that high or higher.Lead poisoning can result in nervous system injury, brain damage, seizures or convulsions, growth or mental retardation, coma and even death for young children.ย While high levels of lead exposure are often the focus of scientists, recent research has highlighted the effects of even low levels of exposure to lead on children. Other studies have tied low lead exposure to the development of kidney damage and depression and panic disorders. Tags: Brain Damage, Children, Lead, Lead Exposure, Lead PoisoningMore Lawsuit Stories Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism July 7, 2026 Omnipod Class Action Lawsuit Filed Over Recalled Insulin Delivery System July 7, 2026 Lack of Safety Features Led to Roblox Child Exploitation, Lawsuit Claims July 7, 2026 1 Comments Julie April 2, 2011 Why are corporations in the US importing from Pakistan anyways… smh! 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This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: today)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026) Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration (Posted: yesterday)A Texas man’s lawsuit claims the electrodes and battery of an Abbott spinal cord stimulator tried to push out of his skin, resulting in a severe infection and the need for surgical removal.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026)Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026) Olympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (Posted: 5 days ago)Federal warnings and enforcement actions involving Olympus and other reusable medical scopes have raised concerns that design flaws may allow bacteria to remain trapped after cleaning, leading to serious infections and product liability lawsuits.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)
Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism July 7, 2026
Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: today)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)
Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration (Posted: yesterday)A Texas man’s lawsuit claims the electrodes and battery of an Abbott spinal cord stimulator tried to push out of his skin, resulting in a severe infection and the need for surgical removal.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026)Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026)
Olympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (Posted: 5 days ago)Federal warnings and enforcement actions involving Olympus and other reusable medical scopes have raised concerns that design flaws may allow bacteria to remain trapped after cleaning, leading to serious infections and product liability lawsuits.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems (03/27/2026)